EC Number |
Inhibitors |
Structure |
---|
1.11.1.7 | 1,10-phenanthroline |
69% inhibition at 5 mM |
|
1.11.1.7 | 1-(5-fluoro-1H-indol-3-yl)methanamine |
- |
|
1.11.1.7 | 1-butyl-3-methylimidazolium tetrafluoroborate |
weak, non-competitive inhibitor |
|
1.11.1.7 | 1-methyl-L-tryptophan |
- |
|
1.11.1.7 | 2,2'-bipyridyl |
25% inhibition at 5 mM |
|
1.11.1.7 | 2,4,6-tribromophenol |
substrate inhibition at high concentration due to the internal binding at the distal pocket of DHP; substrate inhibition at high concentration due to the internal binding at the distal pocket of DHP |
|
1.11.1.7 | 2,4,6-Trichlorophenol |
substrate inhibition at high concentration due to the internal binding at the distal pocket of DHP; substrate inhibition at high concentration due to the internal binding at the distal pocket of DHP |
|
1.11.1.7 | 2,4-dinitroresorcinol |
competitive inhibition of 3,3',5,5'-tetramethylbenzidine oxidation |
|
1.11.1.7 | 2-(5-fluoro-1H-indol-3-yl)-N,N-dimethylethanamine |
- |
|
1.11.1.7 | 2-(5-fluoro-1H-indol-3-yl)-N-methylethanamine |
- |
|